Hasil Pencarian
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DPY19L2 gene mutations are a major cause of globozoospermia: identification of three novel point mutations
No. Panggil: MHR Basic science of reproductive medicine; Volume 19, No.6, June 2013: p.395–404 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development
No. Panggil: MHR Basic science of reproductive medicine; Volume 21, No.2, February 2015: p.169–185 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Subcellular localization of phospholipase Cz in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation
No. Panggil: MHR Basic science of reproductive medicine; Volume 21, No.2, February 2015: p.157–168 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers
No. Panggil: MHR Basic science of reproductive medicine; Volume 20, No.9, September 2014: p.827–835 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Updated overall survival results from a randomized phase III trial comparing gefitinib with carboplatin–paclitaxel for chemo-naïve non-small cell lung cancer with sensitive EGFR gene mutations (NEJ002)
No. Panggil: Annals of Oncology; Volume 24, No.1, January 2013, p54-59 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Male-driven de novo mutations in haploid germ cells
No. Panggil: MHR Basic science of reproductive medicine; Volume 19, No.8, August 2013: p.495–499 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian population
No. Panggil: Neophorlogy Dialysis Transplantation; Volume 29, No.10, October 2014: p.1902–1909 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activity
No. Panggil: Cardiovascular Research; Volume 97, No.1, January 2013, p.44-54 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia
No. Panggil: Neophorlogy Dialysis Transplantation; Volume 28, No.1, January 2013: p.227–232 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
A novel and simple mixture as point-of-use water treatment agent to produce safe drinking water
No. Panggil: Transactions of The Royal Society of Tropical Medicine and Hygiene;Volume 108 No.5 May 2014 p 290–296 |
Koleksi: Artikel Internasional - Oxford  :: Cari yang mirip  :: Tambahkan ke Favorit  ::
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